Evidence map›Paper›PMID 26582957›Full record

ArticleThe Journal of infectious diseases2016

Evolutionarily Successful Asian 1 Dengue Virus 2 Lineages Contain One Substitution in Envelope That Increases Sensitivity to Polyclonal Antibody Neutralization.

Chunling Wang, Leah C Katzelnick, Magelda Montoya, Kien Duong Thi Hue, Cameron P Simmons, Eva Harris

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Envelope domain III EJournal of virology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Understanding dengue virus evolution to support epidemic surveillance and counter-measure development.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2018
    Review
  9. Article
  10. Review
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 4 countries.

Chunling WangDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley.
Leah C KatzelnickDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley Department of Zoology, Center for Pathogen Evolution, University of Cambridge.
Magelda MontoyaDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley.
Kien Duong Thi HueCentre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, United Kingdom Oxford University Clinical Research Unit, Center for Tropical Medicine, Ho Chi Minh City, Vietnam.
Cameron P SimmonsCentre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, United Kingdom Oxford University Clinical Research Unit, Center for Tropical Medicine, Ho Chi Minh City, Vietnam Department of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute, Australia.
Eva HarrisDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley.
University of California, Berkeley · USUniversity of Cambridge · GBUniversity of Melbourne · AUUniversity of Oxford · GB

Funding

Epidemiological, Clinical & Immunological Studies of Zika, dengue and chikungunyaR01AI099631 · NIAID · SUSTAINABLE SCIENCES INSTITUTE · PI BALMASEDA, ANGEL LAZARO · 2012 to 2021
$1.8M
NIAID NIH HHS R01 AI099631
6 · The paper itself

Abstract

The 4 dengue virus serotypes (DENV-1-4) cause the most prevalent mosquito-borne viral disease of humans worldwide. DENV-2 Asian 1 (A1) genotype viruses replaced the Asian-American (AA) genotype in Vietnam and Cambodia, after which A1 viruses containing Q or M at envelope (E) residue 160 became more prevalent than those with residue 160K in both countries (2008-2011). We investigated whether these substitutions conferred a fitness advantage by measuring neutralizing antibody titer against reporter virus particles (RVPs) representing AA, A1-160K, A1-160Q, and A1-160M, using patient sera from Vietnam and a well-characterized Nicaraguan cohort. Surprisingly, we found that A1-160Q and A1-160M RVPs were better neutralized by heterologous antisera than A1-160K. Despite this, Vietnamese patients infected with A1-160Q or A1-160M viruses had higher viremia levels than those infected with A1-160K. We thus found that independent lineages in Vietnam and Cambodia acquired a substitution in E that significantly increased polyclonal neutralization but nonetheless were successful in disseminating and infecting human hosts.

Indexed as

Amino Acid SubstitutionAntibodies, NeutralizingAntibodies, ViralBiological EvolutionCloning, MolecularDengueDengue VirusEvolution, MolecularGene Expression Regulation, ViralHumansPhylogenySerotypingViral Envelope ProteinsAntibodies, NeutralizingAntibodies, ViralViral Envelope ProteinsCambodiadengue virusenvelope proteinevolutionfitnessgenotypelineageneutralizing antibodiesVietnam

Identifiers

PMID26582957
PMCPMC4760423
OpenAlexW2255837968

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.